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GMP

GMP involves manufacturing the products in a way to get quality products while following the Guidelines. The guidelines related to good manufacturing practices will be updated regularly in this section.

  • Usage of Expired Raw Materials to Manufacture Drug
  • Site Acceptance Test (SAT)
  • 3 Types of Airlocks and its Purpose and applications
  • Granulation Technique in tablet manufacturing
  • Deviation, Types of Deviations in Pharmaceuticals
  • Change Control in Pharma, Classification: What it is?
  • WHO-GMP Document Check List for Visitors
  • Role of IPQA during Line Clearance
  • Lean Six Sigma in Pharmaceuticals
  • What is GMP ­­­| cGMP | GMP Principle
  • Contamination and Cross-contamination in Manufacturing
  • Difference between Static and Dynamic Pass box
  • Good Documentation Practice (GDP) in pharmaceuticals
  • GxP in Pharmaceuticals industries (FDA guidelines)
  • Difference between Validation, Calibration, and Qualification in Pharma
  • CAPA Corrective and preventive action in Pharmaceutical
  • Handling of Laboratory Incident in Pharma
  • SOP on Storage and Hold time study for Products
  • Factory Acceptance Test (FAT) in Pharmaceutical
  • Lux or Light intensity standards in pharma industry
  • Stainless Steel Types in Pharmaceutical (Detailed Study)
  • Line Clearance Checklist point production/packing

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